Vang O, Jensen M B, Autrup H
Laboratory of Environmental Carcinogenesis. Fibiger Institute, Danish Cancer Society, Copenhagen.
Carcinogenesis. 1990 Aug;11(8):1259-63. doi: 10.1093/carcin/11.8.1259.
It is known that consumption of cruciferous vegetables protects against the chemical induction of cancer in many organs. It has been suggested that this protection is mediated through an effect on the cytochrome P450 monooxygenase system. This system is responsible for the activation of a number of chemical carcinogens to their ultimate forms. In the present study, the effect of indole-3-carbinol (I3C) and 5,6-benzoflavone (5,6BF) on the expression of cytochrome P450IA1 in rat colon and liver has been investigated. Cytochrome P450IA1 mRNA was induced in colon following a single oral administration of I3C or 5,6BF. A biphasic induction profile was obtained with maxima at 4 and 16 h post-administration. Both inducers caused an approximately 2-fold increase in P450IA1 mRNA at 4 h and a 10-fold increase at 16 h. In contrast, both cytochrome P450IA1 and IA2 mRNAs was increased over the control between 4 and 24 h. The total amount of P450IA mRNAs in liver at 4 and 16 h was increased about 2- and 4-fold respectively by I3C; 5,6BF induced the P450IA mRNAs 4- and 5-fold respectively. The expression of cytochrome P450IA1 and IA2 is induced by I3C and several flavones present in cruciferous vegetables. This suggests that one of the protective effects of cruciferous vegetables in the reduction of chemically induced cancer may be regulation of cytochrome P450s involved in the metabolism of the chemical carcinogens.
已知食用十字花科蔬菜可预防多种器官的化学诱导性癌症。有人提出,这种保护作用是通过对细胞色素P450单加氧酶系统的影响来介导的。该系统负责将多种化学致癌物激活为其最终形式。在本研究中,研究了吲哚 - 3 - 甲醇(I3C)和5,6 - 苯并黄酮(5,6BF)对大鼠结肠和肝脏中细胞色素P450IA1表达的影响。单次口服I3C或5,6BF后,结肠中细胞色素P450IA1 mRNA被诱导。给药后4小时和16小时出现双相诱导曲线,峰值出现。两种诱导剂在给药后4小时使P450IA1 mRNA增加约2倍,在16小时增加10倍。相比之下,在4至24小时内,细胞色素P450IA1和IA2 mRNA均比对照增加。I3C使肝脏中4小时和16小时的P450IA mRNA总量分别增加约2倍和4倍;5,6BF分别诱导P450IA mRNA增加4倍和5倍。细胞色素P450IA1和IA2的表达由I3C和十字花科蔬菜中存在的几种黄酮诱导。这表明十字花科蔬菜在减少化学诱导性癌症方面的保护作用之一可能是调节参与化学致癌物代谢的细胞色素P450。